Cyclopropylboronic acid → (5-Cyclopropyl-2,4-dimethyl-phenyl)-acetic acid methyl ester
反応式
[CH3:1][O:2][C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[C:9](Br)[C:8]([CH3:12])=[CH:7][C:6]=1[CH3:13].[CH:15]1(B(O)O)[CH2:17][CH2:16]1>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:1][O:2][C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[C:9]([CH:15]2[CH2:17][CH2:16]2)[C:8]([CH3:12])=[CH:7][C:6]=1[CH3:13]参加物
5
実験手順
To a solution of 6.0 g of (5-bromo-2,4-dimethyl-phenyl)-acetic acid methyl ester (WO99/48869) in 100 ml of toluene was added 2,2 g of cyclopropylboronic acid and 20 g of potassium phosphate tribasic trihydrate at room temperature. The reaction mixture was stirred for 5 minutes under nitrogen atmosphere, followed by further addition of 1.2 g of tetrakis(triphenylphosphine)palladium(0). After heating and stirring for 16 hours at 110° C., the reaction mixture was filtered, the solvent removed in vacuo and the residue was subjected to silica gel chromatography (isohexane/diethyl ether 2:1) to yield 2.5 g of (5-cyclopropyl-2,4-dimethyl-phenyl)-acetic acid methyl ester.
後処理
- temperatureAfter heating
- stirringstirring for 16 hours at 110° C.
- filtrationthe reaction mixture was filtered
- customthe solvent removed in vacuo
出典と根拠
- ORDレコード
- ord-4a0a069cb427426eaa4e6c5606307325
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08415369B2
反応ノート
読み込み中…